FoodFeb 18, 2026
Karison brand BESAN LADDOO recall — FDA H-0505-2026
Product contains milk, which is undeclared in the ingredient statement.
Class IIFDA: TerminatedKarison Foods & Snacks, Inc.
February 2026 recalls — page 6
These records include useful source details for the selected month.
FoodFeb 18, 2026
Ventura Foods CREAMY PEANUT BUTTER NET WT 1.12 OZ recall — FDA H-0503-2026
Foreign material. During production, the firm found pieces of blue plastic in a filter.
Class IIFDA: TerminatedVentura Foods LLC
FoodFeb 18, 2026
TKS Co-pack Manufacturing Aonic Complete His recall — FDA H-0521-2026
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Class IIFDA: CompletedTKS Co-pack Manufacturing, LLC
FoodFeb 18, 2026
Ventura Foods CREAMY PEANUT BUTTER NET WT 1.12 OZ recall — FDA H-0504-2026
Foreign material. During production, the firm found pieces of blue plastic in a filter.
Class IIFDA: TerminatedVentura Foods LLC
FoodFeb 18, 2026
Karison brand PANJIRI recall — FDA H-0509-2026
Product contains milk, which is undeclared in the ingredient statement.
Class IIFDA: TerminatedKarison Foods & Snacks, Inc.
FoodFeb 18, 2026
TKS Co-pack Manufacturing Aonic Complete Hers recall — FDA H-0520-2026
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Class IIFDA: CompletedTKS Co-pack Manufacturing, LLC
FoodFeb 18, 2026
Cacao Art Crunchy Caramel artisan dark chocolate with crunch brown sugar recall — FDA H-0498-2026
Undeclared allergen - milk. Product contains butter; cream is listed as a sub-ingredient of the butter, but milk is not declared in the ingredients or a contains statement.
Class IIFDA: TerminatedCacao Art
FoodFeb 18, 2026
KPCM New York a.) Preema brand Bright Red Food Colour Powder recall — FDA H-0490-2026
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
Class IIFDA: OngoingKPCM New York Inc.
FoodFeb 18, 2026
MG Foods-Compass Group Spicy Breakfast Burrito in a flour tortilla recall — FDA H-0495-2026
foreign material (small hard plastic fragments)
Class IIFDA: TerminatedMG Foods-Compass Group
DrugFeb 18, 2026
Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle recall — FDA D-0306-2026
Tablets/Capsules Imprinted with Wrong ID
Class IIIFDA: OngoingUnichem Pharmaceuticals USA Inc.
DrugFeb 18, 2026
Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per recall — FDA D-0338-2026
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Class IIFDA: OngoingAmerisource Health Services LLC
DrugFeb 18, 2026
UDENYCA recall — FDA D-0353-2026
Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated…
Class IFDA: OngoingMcKesson
VehicleFeb 13, 2026
General Motors control module software recall — NHTSA campaign 26V085000
General Motors, LLC (GM) is recalling certain 2022 Chevrolet Tahoe, Chevrolet Suburban, GMC Yukon, GMC Yukon XL, Cadillac Escalade, and Cadillac Escalade ESV vehicles equipped with 10 Speed…
control module softwareGeneral Motors, LLC
VehicleFeb 12, 2026
Rogue throttlebody/manifold recall — NHTSA campaign 26V081000
Nissan North America, Inc. (Nissan) is recalling certain 2024-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. The gears in the electronic…
throttlebody/manifoldNissan North America, Inc.
VehicleFeb 12, 2026
Rogue hard parts internal/mechanical recall — NHTSA campaign 26V080000
Nissan North America, Inc. (Nissan) is recalling certain 2023-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. Increased temperatures can…
hard parts internal/mechanicalNissan North America, Inc.
VehicleFeb 12, 2026
General Motors control module software recall — NHTSA campaign 26V083000
General Motors, LLC is recalling certain 2020 Chevrolet Silverado 2500, 3500, GMC Sierra 2500, 3500, and 2020-2022 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles that may have been…
control module softwareGeneral Motors, LLC
Medical DeviceFeb 11, 2026
Changchun Wancheng Bio-Electron Co Vivoo Vaginal pH Test recall — FDA Z-1266-2026
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or…
Class IIFDA: OngoingChangchun Wancheng Bio-Electron Co., Ltd.
Medical DeviceFeb 11, 2026
Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recall — FDA Z-1256-2026
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which…
Class IIFDA: OngoingVortex Surgical Inc.
Medical DeviceFeb 11, 2026
Changchun Wancheng Bio-Electron Co Menopause Test Cassette (Urine) recall — FDA Z-1260-2026
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or…
Class IIFDA: OngoingChangchun Wancheng Bio-Electron Co., Ltd.
Medical DeviceFeb 11, 2026
da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System recall — FDA Z-1232-2026
Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was supposed to be used to detect Universal…
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceFeb 11, 2026
Fujirebio Diagnostics Lumipulse G pTau 217 Plasma Immunoreaction Cartridges recall — FDA Z-1302-2026
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to…
Class IIFDA: OngoingFujirebio Diagnostics, Inc.
Medical DeviceFeb 11, 2026
Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050, (5) recall — FDA Z-1309-2026
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became…
Class IIFDA: OngoingETAC A/S
Medical DeviceFeb 11, 2026
Olympus Corporation of the Americas Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recall — FDA Z-1283-2026
Devices which did not undergo thermoforming could deform and lose performance.
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceFeb 11, 2026
Encore Medical EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H, REF: 942-01-36H recall — FDA Z-1234-2026
942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy,…
Class IIFDA: OngoingEncore Medical, LP
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.